PEPD, peptidase D, 5184

N. diseases: 113; N. variants: 36
Disease: Deficiency of prolidase ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606944
rs267606944
Entrez Id: 5184
Gene Symbol: PEPD
PEPD
CUI: C0268532
Disease:
Deficiency of prolidase 		T 0.700 CausalMutation CLINVAR